MHRA MedTech Regs update: Working together to advance safety

In our September MedTech regulations blog, MHRA Head of Diagnostics and General Medical Devices Joseph Burt seeks stakeholder feedback to two surveys and looks ahead to Autumn updates about the Pre-market statutory instrument, an IVD roadmap and the next IMDRF forum Hello again. If you’re anything like me, you’ve probably wondered how the past few months have vanished so quickly!…